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17 Jul 2008, 9:48 pm
The Food and Drug Administration (FDA) has lifted the Salmonella warning on red and Roma tomatoes: FDA officials believe that consumers may enjoy all types of fresh tomatoes available on the domestic market, without concern of becoming infected with Salmonella Saintpaul. [read post]
2 Mar 2015, 10:01 pm
The bill, previously introduced in June 2013, would require the Food and Drug Administration (FDA) to withdraw its approval of medically important antibiotics used for disease prevention or control that are at a high risk of abuse. [read post]
13 Jan 2023, 10:00 am
A Texas federal court Thursday granted the US Food and Drug Administration’s (FDA) motion to dismiss a lawsuit brought against them for authorizing COVID-19 vaccine administration to children. [read post]
14 Feb 2017, 10:00 pm
“In 2015, this one lot of product was distributed to independent pet retail stores in Washington and Maryland, though it has been verified that this lot is no longer on any store shelves,” according to the Against the Grain recall notice on the Food and Drug Administration website. [read post]
15 Dec 2008, 10:37 am
The Food and Drug Administration is holding a public workshop entitled Sentinel Initiative: Structure, Function, and Scope. [read post]
19 Apr 2015, 9:30 pm
Food and Drug Administration (FDA) has long been approving biologics, there was—until recently—no process for approving generic biologics, known as a biosimilars. [read post]
16 Nov 2021, 9:43 am
Food and Drug Administration (FDA), and public health agencies in other states on an ongoing investigation of an outbreak of E. coli O157 infections associated with eating organic baby spinach. [read post]
21 Jun 2015, 10:03 pm
Food and Drug Administration (FDA), which was only recently made public. [read post]
2 Mar 2011, 1:59 am
Food and Drug Administration (FDA), in response to a consumer complaint received by the FDA. [read post]
12 Apr 2016, 8:00 am
Steven Nissan of the Cleveland Clinic, served on the Food and Drug Administration (FDA) advisory panel that voted to approve Xarelto in 2011. [read post]
2 Apr 2014, 11:37 am
On March 25, 2014, the Food and Drug Administration (FDA) published a proposal to amend its regulations governing the classification and reclassification of medical devices. [read post]
8 Aug 2012, 2:59 am
Food and Drug Administration on the agency's new CORE (Coordinated Outbreak Response and Evaluation) teams.When the Coordinated Outbreak Response and Evaluation (CORE) Network was launched last summer, its teams were tested almost immediately, as was the Food and Drug Administration's new approach to outbreaks of foodborne illnesses.It was August 2011 and reports were coming in of people suffering from Listeria monocytogenes. [read post]
1 Aug 2013, 10:00 am
., Board Certified by The Florida Bar in Health Law A California college student left in a small holding cell by the Drug Enforcement Administration (DEA) for five days without food, water, or a toilet has settled his claims for $4.1 million, according to a number of news sources. [read post]
3 Feb 2022, 8:57 pm
Food and Drug Administration announced approval to Mylan Pharmaceuticals for a generic form of Allergan's RESTASIS® (Cyclosporine Ophthalmic Emulsion 0.05%) product for treatment of chronic dry eye. [read post]
1 Aug 2022, 2:18 pm
The notice was specifically targeted to parties proceeding before both the USPTO and Food and Drug Administration (FDA) and was issued in response to urging by Senators to establish interagency communications aimed in part at eliminating so-called drug patent thickets. [read post]
16 Jun 2020, 2:15 pm
On June 1, the Food and Drug Administration (FDA) published a notice in the Federal Register announcing that the agency was establishing a public docket for the receipt of public comments regarding the types of patent information published in the FDA’s Orange Book, a collection of FDA-approved drugs and their therapeutic equivalents designed to improve competition from generic drugmakers. [read post]
15 Apr 2015, 9:59 pm
Food and Drug Administration ("FDA") denied a citizen petition filed by Amgen in which it requested that action be taken to ensure that biosimilar applicants comply with the disclosure and exchange provisions described in the Biologics Price Competition and Innovation Act (“BPCIA”). [read post]
13 Feb 2014, 12:13 pm
The Work Plan also includes numerous reviews involving other HHS agencies, including the Centers for Disease Control and Prevention, the Food and Drug Administration, and the National Institutes of Health. [read post]
28 Mar 2014, 7:47 pm
ACI faculty will help attendees: • Explore the swiftly evolving landscape of Chinese pharmaceutical regulation and law; • Understand the structure and role of the new Chinese Food and Drug Administration (CFDA); • Minimize regulatory risk when doing business in an atmosphere of heightened enforcement in China; • Master the essentials of the CFDA drug and biologic approval process and navigate the burgeoning Chinese biosimilars market; •… [read post]
5 Jan 2022, 9:44 pm
Food and Drug Administration approved four biosimilar drugs in 2021 under the provisions of the Biologics Price Competition and Innovation Act (BPCIA, codified at 42 U.S.C. [read post]
